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Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare

Myelodysplastic syndromes may be associated with autoimmune diseases. Renal involvement is rare but, if occurs, it manifests predominantly as glomerular diseases. Extramembranous glomerulonephritis associated with myelodysplastic syndrome has been reported very rarely. We here report the case of a p...

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Autores principales: Mehdi, Mahtat El, Alayoude, Ahmed, Hamzi, Mohamed Amine, Arache, Wafe, Hassani, Kawtar, Jennane, Selim, Eddou, Hicham, Doghmi, Kamal, Mikdame, Mohamed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987118/
https://www.ncbi.nlm.nih.gov/pubmed/29875966
http://dx.doi.org/10.11604/pamj.2018.29.85.3486
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author Mehdi, Mahtat El
Alayoude, Ahmed
Hamzi, Mohamed Amine
Arache, Wafe
Hassani, Kawtar
Jennane, Selim
Eddou, Hicham
Doghmi, Kamal
Mikdame, Mohamed
author_facet Mehdi, Mahtat El
Alayoude, Ahmed
Hamzi, Mohamed Amine
Arache, Wafe
Hassani, Kawtar
Jennane, Selim
Eddou, Hicham
Doghmi, Kamal
Mikdame, Mohamed
author_sort Mehdi, Mahtat El
collection PubMed
description Myelodysplastic syndromes may be associated with autoimmune diseases. Renal involvement is rare but, if occurs, it manifests predominantly as glomerular diseases. Extramembranous glomerulonephritis associated with myelodysplastic syndrome has been reported very rarely. We here report the case of a patient presenting with glomerulonephritis associated with anemia, revealing low-risk myelodysplastic syndrome. In the light of this case, we conducted a review of the literature of previously published cases and discussed the pathogenic link between these two entities.
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spelling pubmed-59871182018-06-06 Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare Mehdi, Mahtat El Alayoude, Ahmed Hamzi, Mohamed Amine Arache, Wafe Hassani, Kawtar Jennane, Selim Eddou, Hicham Doghmi, Kamal Mikdame, Mohamed Pan Afr Med J Case Report Myelodysplastic syndromes may be associated with autoimmune diseases. Renal involvement is rare but, if occurs, it manifests predominantly as glomerular diseases. Extramembranous glomerulonephritis associated with myelodysplastic syndrome has been reported very rarely. We here report the case of a patient presenting with glomerulonephritis associated with anemia, revealing low-risk myelodysplastic syndrome. In the light of this case, we conducted a review of the literature of previously published cases and discussed the pathogenic link between these two entities. The African Field Epidemiology Network 2018-01-30 /pmc/articles/PMC5987118/ /pubmed/29875966 http://dx.doi.org/10.11604/pamj.2018.29.85.3486 Text en © Mahtat El Mehdi et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mehdi, Mahtat El
Alayoude, Ahmed
Hamzi, Mohamed Amine
Arache, Wafe
Hassani, Kawtar
Jennane, Selim
Eddou, Hicham
Doghmi, Kamal
Mikdame, Mohamed
Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare
title Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare
title_full Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare
title_fullStr Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare
title_full_unstemmed Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare
title_short Glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare
title_sort glomérulonéphrite extra-membraneuse et syndrome myélodysplasique: une association rare
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5987118/
https://www.ncbi.nlm.nih.gov/pubmed/29875966
http://dx.doi.org/10.11604/pamj.2018.29.85.3486
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